Churchyard A, Donnan G A, Hughes A, Howells D W, Woodhouse D, Wong J Y, Kalnins R M, Mendelsohn F A, Paxinos G
Department of Neurology, Austin Hospital, Victoria, Australia.
Ann Neurol. 1993 Aug;34(2):219-26. doi: 10.1002/ana.410340219.
Postmortem autoradiography was used to explore the mechanisms underlying L-dopa resistance in 2 patients with multiple-system atrophy. Indices of striatal presynaptic dopamine terminal loss and dopamine (D1 and D2) receptors were provided by 3H-mazindol, 3H-SCH 23390, and 125I-sulpiride binding. Neuronal loss, gliosis, and loss of postsynaptic D2 receptors preferentially involved the middle and posterior of the putamen, that region of the striatum most intimately involved in motor function. Loss of D1 receptors in the same area occurred in only 1 patient. These findings suggest that in multiple-system atrophy, resistance to L-dopa is due to a loss of putamental D2 receptors. The differential effects on D1 and D2 receptors in 1 patient implies that different subpopulations of striatal neurons were selectively involved.
采用死后放射自显影术探究2例多系统萎缩患者对左旋多巴耐药的潜在机制。通过3H-吗茚酮、3H-SCH 23390和125I-舒必利结合来提供纹状体突触前多巴胺终末丢失及多巴胺(D1和D2)受体的指标。神经元丢失、胶质增生和突触后D2受体丢失主要累及壳核中部和后部,该区域是纹状体中与运动功能关系最为密切的部分。仅1例患者该区域出现D1受体丢失。这些发现表明,在多系统萎缩中,对左旋多巴耐药是由于壳核D2受体丢失。1例患者中D1和D2受体的不同效应提示,纹状体神经元的不同亚群被选择性累及。